22 results
·
27ms
·
Sources: EU EUDAMED, US FDA
VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)
FDA 510(k)
FDA Unclassified
·Unknown
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613327370751·FACIAL ID-RECON-8PLATES
Zavation
FDA UDI
Zavation LLC·00197157002213·4.5mm Cannulated Tap
Zavation
FDA UDI
Zavation LLC·00197157002268·9.5mm Cannulated Tap
Zavation
FDA UDI
Zavation LLC·00197157002237·6.5mm Cannulated Tap
Zavation
FDA UDI
Zavation LLC·00197157002251·8.5mm Cannulated Tap
Zavation
FDA UDI
Zavation LLC·00197157002220·5.5mm Cannulated Tap
Zavation
FDA UDI
Zavation LLC·00197157002244·7.5mm Cannulated Tap
iLab Polaris Multi-Modality Guidance System
FDA 510(k)
FDA Class 2
·Cardiovascular
STOCKERT CENTRIFUGAL PUMP PLUS SYSTEM (SCP PLUS), MODELS 60-00-10, 60-00-55
FDA 510(k)
FDA Class 2
·Cardiovascular
ILAB POLARIS MULTI-MODALITY GUIDANCE SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQK·March 3, 2025
Persona®
FDA UDI
Zimmer, Inc.·00889024560482·
Persona®
FDA UDI
Zimmer, Inc.·00889024560260·
Persona®
FDA UDI
Zimmer, Inc.·00889024557833·
VerSys®
FDA UDI
Zimmer, Inc.·00889024140394·
VerSys®
FDA UDI
Zimmer, Inc.·00889024140387·
SCREWDRIVER SHAFT, COMPRESSION T2 TIBIA 3.5 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code HXX·July 27, 2012
ILAB? POLARIS MULTI-MODALITY GUIDANCE SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQK·May 14, 2026
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·January 31, 2014
VOYAGER NC CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code LOX·October 29, 2010